Room temperature blue-light emitting liquid crystalline materials based on Phenanthroimidazole substituted Carbazole derivatives

2021 ◽  
Author(s):  
Vinay Kumar Sharma ◽  
Anuj Sharma ◽  
Vekata Subba Rao Ganga ◽  
Pranav Shrivastav ◽  
Priyanka A Jain ◽  
...  

A new class of highly efficient blue emitters consisting of phenanthroimidazole-carbazole hybrid disc shaped molecules with two Schiff base units have been designed and well characterized. All the prepared materials...

2019 ◽  
Vol 1 (9) ◽  
pp. 1959-1969 ◽  
Author(s):  
Vinod Kumar Vishwakarma ◽  
Subrata Nath ◽  
Monika Gupta ◽  
Deepak Kumar Dubey ◽  
Sujith Sudheendran Swayamprabha ◽  
...  

2021 ◽  
Author(s):  
Benedikt Grau ◽  
Maximilian Dill ◽  
Frank Hampel ◽  
Axel Kahnt ◽  
Norbert Jux ◽  
...  

Hexaarylbenzene (HAB) derivatives are versatile aromatic systems playing a significant role as chromophores, liquid crystalline materials, molecular receptors, redox materials, organic light-emitting diodes and photochemical switches. Statistical synthesis of simple symmetrical HABs is known <i>via</i> low-yielding cyclotrimerization or Diels-Alder reactions. By contrast, the synthesis of more complex, asymmetrical systems, and without involvement of statistical steps, remains an unsolved problem. Here we present a generally applicable synthetic strategy to access asymmetrical HAB <i>via</i> an atom-economical and high-yielding metal-free four-step domino reaction using nitrostyrenes and <i>α,α</i>-dicyanoolefins as easily available starting materials. Resulting domino product – functionalized triarylbenzene (TAB) - can be used as a key starting compound to furnish asymmetrically substituted hexaarylbenzenes in high overall yield and without involvement of statistical steps. This straightforward domino process represents a distinct approach to creating diverse and still unexplored HAB scaffolds, containing six different aromatic rings around central benzene core.


Polyhedron ◽  
2011 ◽  
Vol 30 (6) ◽  
pp. 1040-1047 ◽  
Author(s):  
Chira R. Bhattacharjee ◽  
Gobinda Das ◽  
Pankaj Goswami ◽  
Paritosh Mondal ◽  
Subbarao Krishna Prasad ◽  
...  

Synlett ◽  
2011 ◽  
Vol 2011 (14) ◽  
pp. 2104-2104
Author(s):  
Henning Hopf ◽  
Peter Jones ◽  
Zakir Hussain ◽  
Rajeev Menon ◽  
Vitaly Raev ◽  
...  

2006 ◽  
Vol 2006 (24) ◽  
pp. 5555-5569 ◽  
Author(s):  
Zakir Hussain ◽  
Henning Hopf ◽  
Ludwig Pohl ◽  
Thomas Oeser ◽  
Axel K. Fischer ◽  
...  

2021 ◽  
Author(s):  
Benedikt Grau ◽  
Maximilian Dill ◽  
Frank Hampel ◽  
Axel Kahnt ◽  
Norbert Jux ◽  
...  

Hexaarylbenzene (HAB) derivatives are versatile aromatic systems playing a significant role as chromophores, liquid crystalline materials, molecular receptors, redox materials, organic light-emitting diodes and photochemical switches. Statistical synthesis of simple symmetrical HABs is known <i>via</i> low-yielding cyclotrimerization or Diels-Alder reactions. By contrast, the synthesis of more complex, asymmetrical systems, and without involvement of statistical steps, remains an unsolved problem. Here we present a generally applicable synthetic strategy to access asymmetrical HAB <i>via</i> an atom-economical and high-yielding metal-free four-step domino reaction using nitrostyrenes and <i>α,α</i>-dicyanoolefins as easily available starting materials. Resulting domino product – functionalized triarylbenzene (TAB) - can be used as a key starting compound to furnish asymmetrically substituted hexaarylbenzenes in high overall yield and without involvement of statistical steps. This straightforward domino process represents a distinct approach to creating diverse and still unexplored HAB scaffolds, containing six different aromatic rings around central benzene core.


2017 ◽  
Vol 53 (47) ◽  
pp. 6339-6342 ◽  
Author(s):  
Mathieu Ciancone ◽  
Franck Camerel

Laser irradiation allows rapid high temperature phase transition directly from room temperature in pure liquid crystalline materials built around photothermal cores with a high spatial control and responsivness.


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